Provided is a solid electrolyte material represented by a composition formula li3−3δY1+δ−aMaCl6−x−yBrxIy, where M is at least one element selected from the group consisting of Al, Sc, Ga, and Bi; −1<δ<1; 0<a<2; 0<(1+δ−a); 0≤x≤6; 0≤y≤6; and (x+y)≤6.
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9. A solid electrolyte material represented by a composition formula li3−3δY1+δ−a MaCl6−x−yBrxIy,
where
M is at least one element selected from the group consisting of Al, Ga, and Bi;
−1<δ<1;
0<a<2;
0<(1+δ−a);
0≤x≤6;
0≤y≤6; and
(x+y)≤6.
1. A solid electrolyte material represented by a composition formula li3−3δY1+δ−aMaCl6−x−yBrxIy,
where
M is at least one element selected from the group consisting of Al, Sc, Ga, and Bi;
−1<δ<1;
0<a<2;
0<(1+δ−a);
0≤x≤6;
0≤y≤6; and
(x+y)<6, and
wherein an ion conductivity of the solid electrolyte material is not less than 1×10−5 S/cm and not more than 3.0×10−3 S/cm at room temperature.
6. A battery, comprising:
the solid electrolyte material according to
a positive electrode;
a negative electrode; and
an electrolyte layer provided between the positive electrode and the negative electrode,
wherein
at least one selected from the group consisting of the positive electrode, the negative electrode, and the electrolyte layer includes the solid electrolyte material.
7. The solid electrolyte material according to
M is at least one element selected from the group consisting of Al, Ga, and Bi.
14. A battery, comprising:
the solid electrolyte material according to
a positive electrode;
a negative electrode; and
an electrolyte layer provided between the positive electrode and the negative electrode,
wherein
at least one selected from the group consisting of the positive electrode, the negative electrode, and the electrolyte layer includes the solid electrolyte material.
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The present disclosure relates to a solid electrolyte material and a battery.
Patent Literature 1 discloses an all-solid battery using a sulfide solid electrolyte.
Non-Patent Literature 1 discloses Li3YCl6.
Non-Patent Literature 2 discloses Li3YBr6.
In the prior art, realization of a solid electrolyte material having high lithium ion conductivity is desired.
The solid electrolyte material in one aspect of the present disclosure is represented by a composition formula Li3−3δY1+δ−aMaCl6−x−yBrxIy,
where
M is at least one element selected from the group consisting of Al, Sc, Ga, and Bi;
−1<δ<1;
<a<2;
0<(1+δ−a);
0≤x≤6;
0≤y≤6; and
(x+y)≤6.
According to the present disclosure, a solid electrolyte material having high lithium ion conductivity can be realized.
Hereinafter, embodiments of the present disclosure will be described with reference to the drawings.
The solid electrolyte material in the first embodiment is a solid electrolyte material represented by the following composition formula (1):
Li3−3δY1+δ−aMaCl6−x−yBrxIy Formula (1)
where M is one or more kinds of elements selected from the group consisting of Al, Sc, Ga, and Bi.
Further,
−1<δ<1;
0<a<2;
0<(1+δ−a);
0≤x≤6;
0≤y≤6; and
(x+y)≤6 are satisfied.
According to the above configuration, a solid electrolyte material (halide solid electrolyte material) having high lithium ion conductivity can be realized.
In addition, according to the above configuration, an all-solid secondary battery excellent in a charge/discharge characteristic can be realized by using the solid electrolyte material of the first embodiment. In addition, by using the solid electrolyte material of the first embodiment, an all-solid secondary battery which does not including sulfur can be realized. In other words, the solid electrolyte material of the first embodiment does not have a configuration (for example, the configuration of Patent Literature 1) in which hydrogen sulfide is generated when exposed to the atmosphere. For this reason, an all-solid secondary battery which does not generate hydrogen sulfide and is excellent in safety can be realized.
In addition, the solid electrolyte material in the first embodiment may satisfy 0.025≤a≤0.99 in the above composition formula (1).
According to the above configuration, a solid electrolyte material having higher lithium ion conductivity can be realized.
In addition, the solid electrolyte material in the first embodiment may satisfy 0.035≤a≤0.1 in the above composition formula (1).
According to the above configuration, a solid electrolyte material having higher lithium ion conductivity can be realized.
The solid electrolyte material in the first embodiment may satisfy −0.5≤δ≤0.5 in the above composition formula (1).
According to the above configuration, a solid electrolyte material having higher lithium ion conductivity can be realized.
The solid electrolyte material in the first embodiment may satisfy −0.3≤δ≤0.2 in the above composition formula (1).
According to the above configuration, a solid electrolyte material having higher lithium ion conductivity can be realized.
The solid electrolyte material in the first embodiment may be crystalline or amorphous.
In addition, a shape of the solid electrolyte material in the first embodiment is not specifically limited, for example, an acicular shape, a spherical shape, or an elliptical spherical shape. For example, the solid electrolyte material in the first embodiment may be particles. After a plurality of the particles are stacked, the plurality of the particles may be formed into a pellet shape or a plate shape by pressurization.
For example, if the shape of the solid electrolyte material in the first embodiment is particulate (for example, spherical), the median diameter thereof may be not less than 0.1 μm and not more than 100 μm.
In the first embodiment, the median diameter may be not less than 0.5 μm and not more than 10 μm.
According to the above configuration, ion conductivity can be further improved. In addition, a better dispersion state of the solid electrolyte material and the active material in the first embodiment can be formed.
In the first embodiment, the solid electrolyte material may be smaller than the median diameter of the active material.
According to the above configuration, a better dispersion state of the solid electrolyte material and the active material in the first embodiment can be formed.
<Manufacturing Method of Solid Electrolyte Material>
The solid electrolyte material in the first embodiment may be manufactured by the following method, for example.
Binary halide raw material powders are prepared so as to provide a blending ratio of a target composition. For example, if Li3Y0.95Bi0.05Cl6 is produced, LiCl, YCl3, and BiCl3 are prepared at a molar ratio of approximately 3:0.95:0.05. In consideration of change in composition during synthesis process, the blending ratio may be adjusted in advance so as to cancel the change. The above-described values “δ”, “a”, “x”, and “y” can be adjusted by adjusting the raw material, the blending ratio, and the synthesis process.
After the raw material powders are mixed well, the raw material powders are mixed and ground to react by a mechanochemical milling method. Subsequently, the powders may be sintered in a vacuum or an inert atmosphere.
Alternatively, the raw material powders may be mixed well and then sintered in a vacuum or in an inert atmosphere. For example, it is preferable that the powders are sintered within a range of 100° C. to 650° C. for 1 hour or longer.
Thereby, the solid electrolyte material including the composition as described above is provided.
Hereinafter, the second embodiment will be described. The description which has been set forth in the first embodiment is omitted as appropriate.
The battery in the second embodiment is configured using the solid electrolyte material described in the first embodiment.
The battery in the second embodiment comprises a solid electrolyte material, a positive electrode, a negative electrode, and an electrolyte layer.
The electrolyte layer is a layer provided between the positive electrode and the negative electrode.
At least one of the positive electrode, the electrolyte layer, and the negative electrode includes the solid electrolyte material in the first embodiment.
According to the above configuration, the charge/discharge characteristic of the battery can be improved.
A specific example of the battery in the second embodiment will be described below.
The battery 1000 in the second embodiment comprises a positive electrode 201, a negative electrode 203, and an electrolyte layer 202.
The positive electrode 201 includes positive electrode active material particles 204 and solid electrolyte particles 100.
The electrolyte layer 202 is disposed between the positive electrode 201 and the negative electrode 203.
The electrolyte layer 202 includes an electrolyte material (for example, a solid electrolyte material).
The negative electrode 203 includes negative electrode active material particles 205 and solid electrolyte particles 100.
Each of the solid electrolyte particles 100 is a particle formed of the solid electrolyte material in the first embodiment or a particle including the solid electrolyte material in the first embodiment as a main component.
The positive electrode 201 includes a material having a property of storing and releasing metal ions (for example, lithium ions). The positive electrode 201 includes, for example, a positive electrode active material (for example, the positive electrode active material particles 204).
Examples of the positive electrode active material include lithium-containing transition metal oxides (e.g., Li(NiCoAl)O2 or LiCoO2), transition metal fluorides, polyanions, fluorinated polyanion materials, transition metal sulfides, transition metal oxyfluorides, transition metal oxysulfides, and transition metal oxynitrides.
The median diameter of the positive electrode active material particles 204 may be not less than 0.1 μm and not more than 100 μm. If the median diameter of the positive electrode active material particles 204 is less than 0.1 μm, there is a possibility that the positive electrode active material particles 204 and the halide solid electrolyte material cannot form a good dispersion state in the positive electrode. As a result, the charge/discharge characteristic of the battery is lowered. In addition, if the median diameter of the positive electrode active material particles 204 is more than 100 μm, lithium diffusion in the positive electrode active material particles 204 is made slow. As a result, it may be difficult to operate the battery at a high output.
The median diameter of the positive electrode active material particles 204 may be larger than the median diameter of the halide solid electrolyte material. Thereby, the good dispersion state of the positive electrode active material particles 204 and the halide solid electrolyte material can be formed.
With regard to the volume ratio “v:100-v” between the positive electrode active material particles 204 and the halide solid electrolyte material included in the positive electrode 201, 30≤v≤95 may be satisfied. If v<30, it may be difficult to ensure an energy density of the battery sufficiently. In addition, if v>95, it may be difficult to operate at high output.
The thickness of the positive electrode 201 may be not less than 10 μm and not more than 500 μm. If the thickness of the positive electrode is less than 10 μm, it may be difficult to ensure an energy density of the battery sufficiently. In addition, if the thickness of the positive electrode is more than 500 μm, it may be difficult to operate at a high output.
The electrolyte layer 202 is a layer including an electrolyte material. The electrolyte material is, for example, a solid electrolyte material. In other words, the electrolyte layer 202 may be a solid electrolyte layer.
The solid electrolyte layer may include the solid electrolyte material in the first embodiment as a main component. In other words, the solid electrolyte layer may include the solid electrolyte material in the first embodiment, for example, at a weight ratio of not less than 50% (not less than 50% by weight) with respect to the entire solid electrolyte layer.
According to the above configuration, the charge/discharge characteristic of the battery can be further improved.
In addition, the solid electrolyte layer may include the solid electrolyte material in the first embodiment, for example, at a weight ratio of not less than 70% (not less than 70% by weight) with respect to the entire solid electrolyte layer.
According to the above configuration, the charge/discharge characteristic of the battery can be further improved.
The solid electrolyte layer, which may include the solid electrolyte material in the first embodiment as a main component, may further include inevitable impurities. The solid electrolyte layer may include the starting materials used for the synthesis of the solid electrolyte material. The solid electrolyte layer may include by-products or decomposition products generated when the solid electrolyte material is synthesized.
In addition, the solid electrolyte layer may include the solid electrolyte material in the first embodiment, for example, at a weight ratio of 100% (100% by weight) to the entire solid electrolyte layer, except for the inevitable impurities.
According to the above configuration, the charge/discharge characteristic of the battery can be further improved.
As described above, the solid electrolyte layer may be composed only of the solid electrolyte material in the first embodiment.
Alternatively, the solid electrolyte layer may be composed only of a solid electrolyte material different from the solid electrolyte material in the first embodiment. As the solid electrolyte material different from the solid electrolyte material in the first embodiment, for example, Li2MgX4, Li2FeX4, Li(Al, Ga, In)X4, Li3(Al, Ga, In)X6, or LiI(X: Cl, Br, I) may be used.
The solid electrolyte layer may include simultaneously the solid electrolyte material in the first embodiment and the solid electrolyte material different from the solid electrolyte material in the first embodiment. At this time, both of them may be dispersed uniformly. The layer formed of the solid electrolyte material in the first embodiment and the layer formed of the solid electrolyte material different from the solid electrolyte material in the first embodiment may be sequentially arranged in the stacking direction of the battery.
The thickness of the solid electrolyte layer may be not less than 1 μm and not more than 1,000 μm. If the thickness of the solid electrolyte layer is less than 1 μm, the possibility that the positive electrode 201 and the negative electrode 203 are short-circuited increases. In addition, if the thickness of the solid electrolyte layer is more than 1,000 μm, it may be difficult to operate at a high output.
The negative electrode 203 includes a material having a property of storing and releasing metal ions (for example, lithium ions). The negative electrode 203 includes, for example, a negative electrode active material (for example, the negative electrode active material particles 205).
As the negative electrode active material, a metal material, a carbon material, an oxide, a nitride, a tin compound, or a silicon compound may be used. The metal material may be a single metal. Alternatively, the metal material may be an alloy. Examples of the metal material include a lithium metal and a lithium alloy. Examples of the carbon material include natural graphite, coke, graphitized carbon, carbon fiber, spherical carbon, artificial graphite, and amorphous carbon. From the viewpoint of capacity density, silicon (Si), tin (Sn), a silicon compound, or a tin compound may be preferably used. If a negative electrode active material having a low average reaction voltage is used, the effect of suppressing electrolysis by the solid electrolyte material in the first embodiment is better exhibited.
The median diameter of the negative electrode active material particles 205 may be not less than 0.1 μm and not more than 100 μm. If the median diameter of the negative electrode active material particles 205 is less than 0.1 μm, there is a possibility that the negative electrode active material particles 205 and the solid electrolyte particles 100 cannot form a good dispersion state in the negative electrode. Thereby, the charge/discharge characteristic of a battery is lowered. On the other hand, if the median diameter of the negative electrode active material particles 205 is more than 100 μm, lithium diffusion in the negative electrode active material particles 205 is made slow. As a result, it may be difficult to operate the battery at a high output.
The median diameter of the negative electrode active material particles 205 may be larger than the median diameter of the solid electrolyte particles 100. Thereby, the good dispersion state of the negative electrode active material particles 205 and the halide solid electrolyte material can be formed.
With regard to the volume ratio “v:100-v” of the negative electrode active material particles 205 and the solid electrolyte particles 100 included in the negative electrode 203, 30≤v≤95 may be satisfied. If v<30, it may be difficult to ensure an energy density of the battery sufficiently. In addition, if v>95, it may be difficult to operate at high output.
The thickness of the negative electrode 203 may be not less than 10 μm and not more than 500 μm. If the thickness of the negative electrode is less than 10 μm, it may be difficult to ensure an energy density of the battery sufficiently. In addition, if the thickness of the negative electrode is more than 500 μm, it may be difficult to operate at a high output.
At least one of the positive electrode 201, the electrolyte layer 202, and the negative electrode 203 may include a sulfide solid electrolyte or an oxide solid electrolyte for the purpose of improving ion conductivity, chemical stability, or electrochemical stability. As the sulfide solid electrolyte, Li2S—P2S5, Li2S—SiS2, Li2S—B2S3, Li2S—GeS2, Li3.25Ge0.25P0.75S4, or Li10GeP2S12 may be used. As the oxide solid electrolyte, a NASICON solid electrolyte such as LiTi2(PO4)3 and its element substitution products, a (LaLi)TiO3 perovskite solid electrolyte, a LISICON solid electrolyte such as Li14ZnGe4O16, Li4SiO4, LiGeO4 and its element substitution products, a garnet solid electrolyte such as Li7La3Zr2O12 and its element substitution products, Li3N and its H substitution products, and Li3PO4 and its N substitution products may be used.
At least one of the positive electrode 201, the electrolyte layer 202, and the negative electrode 203 may include an organic polymer solid electrolyte for the purpose of increasing ion conductivity. As the organic polymer solid electrolyte, for example, a compound of a polymer compound and a lithium salt can be used. The polymer compound may have an ethylene oxide structure. Due to the ethylene oxide structure, a large amount of lithium salt can be included to further increase the ion conductivity. As the lithium salt, LiPF6, LiBF4, LiSbF6, LiAsF6, LiSO3CF3, LiN(SO2CF3)2, LiN(SO2C2F5)2, LiN(SO2CF3)(SO2C4F9), or LiC(SO2CF3)3 may be used. As the lithium salt, one lithium salt selected from these may be used alone. Alternatively, a mixture of two or more kinds of the lithium salts selected from these may be used as the lithium salt.
At least one of the positive electrode 201, the electrolyte layer 202, and the negative electrode 203 may include a non-aqueous electrolyte solution, a gel electrolyte, or an ionic liquid for the purpose of facilitating exchange of lithium ions and improving the output characteristic of the battery.
The non-aqueous electrolyte solution includes a non-aqueous solvent and a lithium salt dissolved in the non-aqueous solvent. As the non-aqueous solvent, a cyclic carbonate solvent, a chain carbonate solvent, a cyclic ether solvent, a chain ether solvent, a cyclic ester solvent, a chain ester solvent, or a fluorine solvent may be used. Examples of the cyclic carbonate solvent include ethylene carbonate, propylene carbonate, and butylene carbonate. Examples of the chain carbonate solvent include dimethyl carbonate, ethyl methyl carbonate, and diethyl carbonate. Examples of the cyclic ether solvent include tetrahydrofuran, 1,4-dioxane, and 1,3-dioxolane. Examples of the chain ether solvent include 1,2-dimethoxyethane and 1,2-diethoxyethane. Examples of the cyclic ester solvent include γ-butyrolactone. Examples of the chain ester solvent include methyl acetate. Examples of the fluorine solvent include fluoroethylene carbonate, methyl fluoropropionate, fluorobenzene, fluoroethyl methyl carbonate, and fluorodimethylene carbonate. As the non-aqueous solvent, one non-aqueous solvent selected from these may be used alone. Alternatively, a combination of two or more kinds of non-aqueous solvents selected from these may be used as the non-aqueous solvent. The non-aqueous electrolyte solution may include at least one fluorine solvent selected from the group consisting of fluoroethylene carbonate, methyl fluoropropionate, fluorobenzene, fluoroethyl methyl carbonate, and fluorodimethylene carbonate. As the lithium salt, LiPF6, LiBF4, LiSbF6, LiAsF6, LiSO3CF3, LiN(SO2CF3)2, LiN(SO2C2F5)2, LiN(SO2CF3)(SO2C4F9), or LiC(SO2CF3)3 may be used. As the lithium salt, one lithium salt selected from these may be used alone. Alternatively, a mixture of two or more kinds of lithium salts selected from these may be used as the lithium salt. The concentration of the lithium salt is, for example, within a range of 0.5 to 2 mol/liter.
As the gel electrolyte, a polymer material including the non-aqueous electrolyte solution may be used. As the polymer material, polyethylene oxide, polyacrylonitrile, polyvinylidene fluoride, polymethyl methacrylate, or a polymer having an ethylene oxide bond may be used.
The cation forming the ionic liquid may be:
an aliphatic chain quaternary salt such as tetraalkylammonium or tetraalkylphosphonium,
aliphatic cyclic ammonium such as pyrrolidinium, morpholinium, imidazolinium, tetrahydropyrimidinium, piperazinium, or piperidinium; or
a nitrogen-containing heterocyclic aromatic cation such as pyridinium or imidazolium.
An anion forming the ionic liquid is PF6−, BF4−, SbF6−, AsF6−, SO3CF3−, N(SO2CF3)2−, N(SO2C2F5)2−, N(SO2CF3)(SO2C4F9)−, or C(SO2CF3)3−. The ionic liquid may include a lithium salt.
At least one of the positive electrode 201, the electrolyte layer 202, and the negative electrode 203 may include a binder for the purpose of improving the adhesion between the particles. The binder is used to improve the binding property of the material forming the electrode. Examples of the binder include polyvinylidene fluoride, polytetrafluoroethylene, polyethylene, polypropylene, aramid resin, polyamide, polyimide, polyamideimide, polyacrylonitrile, polyacrylic acid, methyl polyacrylate ester, ethyl polyacrylate ester, hexyl polyacrylate ester, polymethacrylic acid, methyl polymethacrylate ester, ethyl polymethacrylate ester, hexyl polymethacrylate ester, polyvinyl acetate, polyvinylpyrrolidone, polyether, polyethersulfone, hexafluoropolypropylene, styrene butadiene rubber, and carboxymethylcellulose. As the binder, a copolymer of two or more kinds of materials selected from tetrafluoroethylene, hexafluoroethylene, hexafluoropropylene, perfluoroalkyl vinyl ether, vinylidene fluoride, chlorotrifluoroethylene, ethylene, propylene, pentafluoropropylene, fluoromethyl vinyl ether, acrylic acid, and hexadiene may be used. In addition, two or more kinds of selected from these may be mixed and used as the binder.
In addition, at least one of the positive electrode 201 and the negative electrode 203 may include a conductive agent as necessary.
The conductive agent is used to reduce electrode resistance. Examples of the conductive agent include graphite such as natural graphite or artificial graphite; carbon black such as acetylene black or ketjen black; a conductive fiber such as a carbon fiber or a metal fiber; carbon fluoride; metal powder such as aluminum; conductive whiskers such as zinc oxide or potassium titanate; a conductive metal oxide such as titanium oxide; or a conductive polymer compound such as polyaniline, polypyrrole, or polythiophene. Cost reduction can be achieved by using such a carbon conductive agent as the conductive agent.
An example of the shape of the battery in the second embodiment is a coin, a cylinder, a prism, a sheet, a button, a flat type, or a stacking structure.
Hereinafter, details of the present disclosure will be described with reference to inventive examples and comparative example.
[Production of Solid Electrolyte Material]
In an argon atmosphere having a dew point of −60° C. or less, raw material powders LiCl, YCl3, and BiCl3 were prepared at a molar ratio of LiCl:YCl3:BiCl3=3:0.95:0.05. These were ground and mixed in a mortar. Subsequently, milling processing was performed at 600 rpm for 25 hours using a planetary ball mill.
In this way, a powder of the solid electrolyte material of the inventive example 1 represented by the composition formula of Li3Y0.95Bi0.05Cl6 was provided.
[Evaluation of Lithium Ion Conductivity]
A pressure-molding die 300 is composed of a frame 301 formed of an electronically insulating polycarbonate, an upper punch part 303 and a lower punch part 302, both of which are formed of electron conductive stainless steel.
Using the configuration shown in
In a dry atmosphere with a dew point of −30° C. or lower, the inside of the pressure-molding die 300 was filled with the powder of the solid electrolyte material of the inventive example 1, and uniaxially pressed at 400 MPa to produce a conductivity measurement cell of the inventive example 1.
In the pressurized state, lead wires were routed from the upper punch part 303 and the lower punch part 302, connected to a potentiostat (Princeton Applied Research, VersaSTAT4) equipped with a frequency response analyzer. The ion conductivity at room temperature was measured by an electrochemical impedance measurement method.
In
The ion conductivity was calculated from the following formula (2) using the resistance value of the electrolyte.
σ=(RSE×S/t)−1 (2)
where σ is ion conductivity, S is an electrolyte area (inner diameter of the frame 301 in
The ion conductivity of the solid electrolyte material of the inventive example 1 measured at 22° C. was 6.3×10−4 S/cm.
[Production of Secondary Battery]
In the argon glove box, the solid electrolyte material of the inventive example 1 and LiCoO2 (hereinafter, referred to as LCO), which was an active material, were prepared at a volume ratio of 70:30. These were mixed in an agate mortar to prepare a mixture.
In an insulating outer cylinder, the solid electrolyte material of the inventive example 1 corresponding to 700 μm thickness, 8.54 mg of the above mixture, and 14.7 mg of Al powder were stacked in this order. This was pressure-molded at a pressure of 300 MPa to provide a first electrode and a solid electrolyte layer.
Next, a metal In (thickness: 200 μm) was stacked on the surface of the solid electrolyte layer opposite to the other surface which was in contact with the first electrode. This was pressure-molded at a pressure of 80 MPa to produce a stacking structure composed of the first electrode, the solid electrolyte layer, and a second electrode.
Next, stainless steel current collectors were placed on the upper and lower parts of the stacking structure, and current collector leads were attached to the current collectors.
Finally, an insulating ferrule was used to block and seal the inside of the insulating outer cylinder from the outside atmosphere.
In this way, the secondary battery of the inventive example 1 was produced.
[Charge/Discharge Test]
The results shown in
In other words, the secondary battery of the inventive example 1 was placed in a thermostatic chamber at 25° C.
The battery was constant-current charged at a current value of 0.05 C rate (20 hour rate) with respect to the theoretical capacity of the battery, and the charge was terminated at a voltage of 3.6 V.
Next, the battery was discharged at a current value of 0.05 C rate, and the discharge was terminated at a voltage of 2.0 V.
As a result of the above measurement, the initial discharge capacity of the secondary battery of the inventive example 1 was 888 μAh.
Hereinafter, the synthesis and evaluation methods of Li3−3δY1+δ−aMaCl6−x−yBrxIy will be described.
[Production of Solid Electrolyte Material]
In the inventive examples 2 to 22, raw material powders were prepared in a glove box maintained in a dry/low oxygen atmosphere having a dew point of −90° C. or less and an oxygen value of 5 ppm or less.
In the inventive examples 2 to 17, raw material powders LiCl, YCl3, and MCl3 were prepared at a molar ratio of LiCl:YCl3:MCl3=(3-3δ):(1+δ−a):a.
In the inventive example 18, raw material powders LiBr, YBr3, and MBr3 were prepared at a molar ratio of LiBr:YBr3:MBr3=(3-3δ):(1+δ−a):a.
In the inventive examples 19 and 20, raw material powders LiCl, YBr3, and MBr3 were prepared at a molar ratio of LiCl:YBr3:MBr3=3:(1−a):a.
In the inventive example 21, raw material powders LiI, YBr3, and MBr3 were prepared at a molar ratio of LiI:YBr3:MBr3=3:0.95:0.05.
In the inventive example 22, raw material powders LiI, LiBr, YCl3, YBr3, and MBr3 were prepared at a molar ratio of LiI:LiBr:YCl3:YBr3:MBr3=2:1:0.6667:0.2833:0.05.
The values of “δ” and “a” and the element of “M” in each of the inventive examples 2 to 22 are shown in Table 1.
The solid electrolyte materials of the inventive examples 2 to 22 were produced in the same manner as in the inventive example 1.
[Evaluation of Lithium Ion Conductivity]
In a glove box maintained in a dry/low oxygen atmosphere with a dew point of −90° C. or less and an oxygen value of 5 ppm or less, each conductivity measurement cell of the inventive examples 2 to 22 was provided in the same manner as in the inventive example 1.
Except for this, ion conductivity was measured in the same manner as in the inventive example 1.
The ion conductivity in each of the inventive examples 2 to 22 is shown in the following Table 1.
[Production of Secondary Battery]
In a glove box maintained in a dry/low oxygen atmosphere with a dew point of −90° C. or less and an oxygen value of 5 ppm or less, each solid electrolyte material of the inventive examples 2 to 22 and LiCoO2, which was a positive electrode active material, were prepared at a volume ratio of 30:70. These were mixed in an agate mortar to produce a positive electrode mixture of each of the inventive examples 2 to 22.
Except for these, the secondary batteries of the inventive examples 2 to 22 were produced in the same manner as in the inventive example 1.
[Charge/Discharge Test]
A charge/discharge test of each of the secondary batteries of the inventive examples 2 to 22 was performed in the same manner as in the inventive example 1.
The initial discharge characteristic of each of the inventive examples 2 to 22 was similar to that of the inventive example 1, and a good charge/discharge characteristic was provided.
LiCl and FeCl2 were used as raw material powders for a solid electrolyte, and mixed at a molar ratio of LiCl:FeCl2=2:1.
Except for this, the synthesis, the evaluation and the analysis were performed in the same manner as in the inventive example 1.
The ion conductivity measured at 22° C. was 9×10−6 S/cm.
In addition, the solid electrolyte material of the inventive example 2 was used as a solid electrolyte used for the mixture and the solid electrolyte layer.
Except for this, a secondary battery was produced and a charge/discharge test was conducted in the same manner as in the inventive example 1.
The initial discharge capacity of the secondary battery of the inventive example was not more than 1 μAh, and the charge/discharge operation failed to be observed.
Table 1 shows each configuration and each evaluation result in the inventive examples 1 to 22 and the comparative example 1.
TABLE 1
Conductivity
Composition
Anion
δ
a
M
(S/m)
Inventive
Li3Y0.95Bi0.05Cl6
Cl
0
0.05
Bi
6.3E−04
Example 1
Inventive
Li3Y0.9Bi0.1Cl6
Cl
0
0.1
Bi
6.0E−04
Example 2
Inventive
Li3Y0.5Bi0.5Cl6
Cl
0
0.5
Bi
1.1E−04
Example 3
Inventive
Li4.5Y0.475Bi0.025Cl6
Cl
−0.5
0.025
Bi
6.4E−05
Example 4
Inventive
Li3.9Y0.665Bi0.035Cl6
Cl
−0.3
0.035
Bi
1.8E−04
Example 5
Inventive
Li2.4Y1.14Bi0.06Cl6
Cl
0.2
0.06
Bi
5.5E−04
Example 6
Inventive
Li1.5Y1.425Bi0.075Cl6
Cl
0.5
0.075
Bi
6.7E−05
Example 7
Inventive
Li3Y0.9Al0.1Cl6
Cl
0
0.1
Al
4.53E−04
Example 8
Inventive
Li3Y0.8Al0.2Cl6
Cl
0
0.2
Al
6.7E−05
Example 9
Inventive
Li3Y0.7Al0.3Cl6
Cl
0
0.3
Al
1.7E−05
Example 10
Inventive
Li3Y0.95Sc0.05Cl6
Cl
0
0.05
Sc
6.3E−04
Example 11
Inventive
Li3Y0.9Sc0.1Cl6
Cl
0
0.1
Sc
5.9E−04
Example 12
Inventive
Li3Y0.7Sc0.3Cl6
Cl
0
0.3
Sc
4.0E−04
Example 13
Inventive
Li3Y0.5Sc0.5Cl6
Cl
0
0.5
Sc
3.3E−04
Example 14
Inventive
Li3Y0.01Sc0.99Cl6
Cl
0
0.99
Sc
1.9E−04
Example 15
Inventive
Li3Y0.95Ga0.05Cl6
Cl
0
0.05
Ga
3.6E−04
Example 16
Inventive
Li3Y0.9Ga0.1Cl6
Cl
0
0.1
Ga
3.8E−04
Example 17
Inventive
Li3Y0.95Bi0.05Br6
Br
0
0.05
Bi
6.2E−04
Example 18
Inventive
Li3Y0.5Sc0.5Cl3Br3
Cl, Br
0
0.5
Sc
3.4E−04
Example 19
Inventive
Li3Y0.95Bi0.05Cl3Br3
Cl, Br
0
0.05
Bi
1.3E−03
Example 20
Inventive
Li3Y0.95Bi0.05Br3I3
Br, I
0
0.05
Bi
6.7E−04
Example 21
Inventive
Li3Y0.95Bi0.05Cl2Br2I2
Cl,
0
0.05
Bi
3.0E−03
Example 22
Br, I
Comparative
Li2FeCl4
Cl
9E−06
Example 1
It can be seen that the inventive examples 1 to 22 show higher ion conductivity of not less than 1×10−5 S/cm in the vicinity of room temperature, as compared to the comparative example 1.
In particular, if a value of a substitution amount a of M defined by the formula (1) is within the range of 0.01≤a≤0.99, higher ion conductivity is exhibited. As is clear from the inventive examples 1 to 3 and 8 to 17, if 0.01≤a≤0.5 is satisfied for M=Bi, if 0.01≤a≤0.1 is satisfied for M=Al, if 0.01≤a≤0.99 is satisfied for M=Sc, or if 0.01≤a≤0.1 is satisfied for M=Ga, higher ion conductivity is exhibited.
Further, if the value of δ, which indicates an amount of Li deficiency from the stoichiometric ratio thereof, is −0.5≤δ≤0.5, higher ion conductivity is exhibited. As is clear from the inventive examples 4 to 7, if the value of δ is within the range of −0.3≤δ≤0.2, higher ion conductivity is exhibited.
In each of the inventive examples 1 to 22, the battery charge/discharge operation was performed at room temperature. On the other hand, in the comparative example 1, the discharge capacity was hardly provided, and the battery operation failed to be observed. Furthermore, since the materials of the inventive examples 1 to 22 do not include sulfur as a constituent element, hydrogen sulfide is not generated.
From the above, it is shown that the solid electrolyte material according to the present disclosure is an electrolyte material that does not generate hydrogen sulfide, exhibits high lithium ion conductivity, and can perform a good charge/discharge operation.
The battery of the present disclosure can be used as, for example, an all solid lithium secondary battery.
Asano, Tetsuya, Sakai, Akihiro, Nishio, Yusuke, Sakaida, Masashi, Miyazaki, Akinobu, Hasegawa, Shinya
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